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Allomyrina dichotoma Larva Extract Ameliorates the Hepatic Insulin Resistance of High-Fat Diet-Induced Diabetic Mice

机译:拟南芥幼虫提取物改善高脂饮食诱导的糖尿病小鼠的肝胰岛素抵抗

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摘要

Allomyrina dichotoma larva is a nutritional-worthy future food resource and it contributes to multiple pharmacological functions. However, its antidiabetic effect and molecular mechanisms are not yet fully understood. Therefore, we investigated the hypolipidemic effect of A. dichotoma larva extract (ADLE) in a high-fat diet (HFD)-induced C57BL/6J mice model. Glucose tolerance and insulin sensitivity in HFD-induced diabetic mice significantly improved after ADLE administration for six weeks. The levels of serum triglyceride (TG), aspartate aminotransferase (AST), alanine transferase (ALT) activity, and lipid accumulation were increased in the liver of HFD-fed mice, but the levels were significantly reduced by the ADLE treatment. Moreover, hepatic fibrosis and inflammatory gene expression in the liver from HFD-treated mice were ameliorated by the ADLE treatment. Dephosphorylation of AMP-activated protein kinase (AMPK) by palmitate was inhibited in the ADLE treated HepG2 cells, and subsequently reduced expression of lipogenic genes, such as SREPBP-1c, ACC, and FAS were observed. The reduced expression of lipogenic genes and an increased phosphorylation of AMPK was also observed in the liver from diabetic mice treated with ADLE. In conclusion, ADLE ameliorates hyperlipidemia through inhibition of hepatic lipogenesis via activating the AMPK signaling pathway. These findings suggest that ADLE and its constituent bioactive compounds are valuable to prevent or treat hepatic insulin resistance in type 2 diabetes.
机译:小夜蛾Allomyrina dichotoma幼虫是一种具有营养价值的未来食品资源,它具有多种药理作用。但是,其抗糖尿病作用和分子机制尚未完全了解。因此,我们在高脂饮食(HFD)诱导的C57BL / 6J小鼠模型中研究了双歧拟南芥幼虫提取物(ADLE)的降血脂作用。服用ADLE六周后,HFD诱导的糖尿病小鼠的葡萄糖耐量和胰岛素敏感性显着改善。在喂食HFD的小鼠肝脏中,血清甘油三酸酯(TG),天冬氨酸转氨酶(AST),丙氨酸转移酶(ALT)活性和脂质蓄积水平增加,但通过ADLE处理后,这些水平显着降低。此外,通过ADLE治疗改善了HFD治疗小鼠肝脏的肝纤维化和炎性基因表达。在ADLE处理的HepG2细胞中,棕榈酸酯对AMP激活的蛋白激酶(AMPK)的去磷酸化作用受到抑制,随后观察到脂肪生成基因(如SREPBP-1c,ACC和FAS)的表达降低。在用ADLE治疗的糖尿病小鼠的肝脏中,也观察到脂肪形成基因的表达减少和AMPK的磷酸化增加。总之,ADLE通过激活AMPK信号通路抑制肝脂生成,从而改善高脂血症。这些发现表明,ADLE及其组成的生物活性化合物对于预防或治疗2型糖尿病的肝胰岛素抵抗是有价值的。

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